Xpert EV - FDA Registration 5e1c5e2452c5a74b46d35de74068d843
Access comprehensive regulatory information for Xpert EV in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5e1c5e2452c5a74b46d35de74068d843 and manufactured by Cepheid. The device was registered on April 05, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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FDA Official Data
5e1c5e2452c5a74b46d35de74068d843
Xpert EV
FDA ID: 5e1c5e2452c5a74b46d35de74068d843
Device Classification
Brand Name
GeneXpert
Registration Information
Analysis ID
5e1c5e2452c5a74b46d35de74068d843
Registration Date
April 05, 2022
Manufacturer
Name
CepheidAuthorized Representative

